The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is characterized by congenital or early-onset camptodactyly, childhood-onset noninflammatory arthropathy …

2023年1月24日 · Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome, caused by biallelic pathogenic mutations in the proteoglycan 4 (PRG4) gene, is characterized by early …

2021年4月1日 · CACP syndrome (OMIM 208250) is a rare autosomal recessive disease characterized by early-onset camptodactyly, noninflammatory arthropathy, progressive coxa …

Background: Camptodactyly-arthropathy-coxavara-pericarditis (CACP) syndrome is a rare autosomal recessive disorder caused by mutations in the gene proteoglycan 4 (PRG4), …

2022年12月4日 · Camptodactyly–arthropathy–coxa vara–pericarditis (CACP) syndrome is a rare genetic disease characterized by tetrad camptodactyly, noninflammatory arthropathy, coxa …

2013年10月1日 · Camptodactyly-arthropathy-coxavara-pericarditis (CACP) syndrome is a rare autosomal recessive disorder caused by mutations in the gene proteoglycan 4 (PRG4), …

The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is an autosomal recessive condition characterized by the association of congenital or early-onset …

2016年5月25日 · CACP syndrome is a rare autosomal recessive disorder characterized by a triad of camptodactyly, childhood non-inflammatory arthropathy with synovial hyperplasia and coxa …

2011年9月14日 · The CACP syndrome is characterized by congenital camptodactyly and early childhood onset of non inflammatory synovial hyperplasia. Some patients present with coxa …

Camptodactyly-Arthropathy-Coxa vara-Pericarditis (CACP) syndrome is a rare autosomal recessive disorder caused by mutations in PRG4 gene that encodes for proteoglycan 4, a …